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Dr. William Mieler, MD
Professor of Ophthalmology and Visual Sciences, University of Illinois, Chicago
Vice Chairman and Director of Ocular Oncology

Thermo-responsive Hydrogels as a New Platform for Drug Delivery to the Posterior Segment of the Eye

Targeted, localized, extended drug delivery to the posterior segment of the eye (retina) poses a number of significant challenges.  This presentation will review our work with thermo-responsive hydrogel delivery of anti-VEGF agents to the retina.  Current treatment of age-related macular degeneration with anti-VEGF agents involves an intravitreal injection of the medication every four to six weeks.  We are working toward a three to six month, non-invasive, drug delivery system.  This presentation will provide an overview of our ongoing work. 

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Dr. Barrett Rabinow, PhD
Baxter Healthcare, Baxter Distinguished Scientist
Director of Strategic Development

Nanoparticles-Impact on PK and Distribution

The nanoparticles that will be discussed are crystalline drug particles, stabilized by surfactant coatings, prepared by a combination of precipitation followed by homogenization. Depending upon its dissolution rate, several pharmacokinetic scenarios can occur upon injection of a drug nanosuspension: 1) the suspension dissolves rapidly, affording pharmacokinetics equivalent to that for an a priori solution formulation, 2) the suspension releases slowly over time, permitting an SC, IM, or ID depot, sustained release dosage form, or 3) the particle suspension in blood does not dissolve quickly, but over a period of minutes traverses the pulmonary circulation, and is then taken up by the spleen and liver. This PK and distribution behavior is similar to that for intravenous injection of any inert particle suspension. This results in rapid uptake of the particles and slow subsequent release by the monocyte phagocytic system, to the extent that the drug can be solubilized within the macrophages. This can dramatically enhance efficacy for drugs whose toxicity is mediated by peak levels but whose efficacy is driven by AUC. Besides pharmacokinetic modification, targeting of nanosuspensions to sites of disease can be managed by harnessing the natural targeting capabilities of macrophages, which migrate to sites of inflammation, infection, and tumor. Case examples will be shown for anti-fungal enhancement of efficacy, anti-neoplastic agent improvement of PK, and targeting of the brain and other viral sanctuaries for treatment of HIV infection in animal models. 



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Dr. Lonnie Shea, PhD
Associate Professor of Chemical and Biological Engineering, Northwestern University

Biomaterials for delivery of gene therapy vectors in regenerative medicine

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Dr. Joseph Wong, PhD
Baxter Healthcare, Principal Scientist


Product Development Considerations with Injectable Nanosuspensions

There has been growing interest in nanoparticles as an approach to formulate poorly soluble drugs. Besides enhanced dissolution rates, and thereby, improved bioavailability, nanoparticles can also provide targeting capabilities when injected intravenously. The latter property has led to increased research and development activities for intravenous suspensions. Additional clinical trials have been conducted or are ongoing for multiple other indications such as oncology and infective diseases. This presentation provides an insight into various challenges associated with developing intravenous nanosuspension dosage forms.  

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Dr. Michael Kaminski, PhD
Argonne National Laboratory, Nuclear Forensics and Nanoscale Engineering Chemical Engineering Division

Magnetic drug delivery technology

Primary obstacles to developing novel drugs are their poor solubility, non-specific targeting, and cytotoxicity. Therefore, adjuvants such as delivery vehicles can become important technologies to improve drug discovery. One such delivery vehicle is magnetic carriers. These are polymeric microspheres or nanospheres that co-encapsulate drug and magnetic nanoparticles. The magnetic susceptibility allows the carriers to be physically-positioned to improve targeting, enables low-level detection by magnetic resonance, and allows drug release profiles to be controlled. The polymeric substrate provides versatile functionality to improve drug carrier circulation, attach specific ligands for targeting, and protect the drug from inactivation by blood-born enzymes. Dr. Kaminski will discuss the state-of-the-art in magnetic drug carriers and activities that his laboratory has been involved.

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04/26/2009  KAT            contact kschwa4@uic.edu regarding this webpage

                                                CRS -- Illinois Student Chapter

 

 

 

 

 

 

 

 

 

 

 

 

Start time

End time

Event

Location

8:00

8:30

Registration

Floor

8:30

8:40

Opening symposium remarks Vice Chancellor Larry Danziger, PharmD., Interim Vice Chancellor for Research at University of Illinois at Chicago

 

Chicago Rm A

8:40

8:43

Opening symposium remarks Dean Jerry Bauman, PharmD., Dean of the University of Illinois at Chicago College of Pharmacy

 

Chicago Rm A

8:43

8:45

Opening symposium remarks Misuk Bae, Chair, CRS -- Illinois Student Chapter

 

Chicago Rm A

8:45

9:30

Keynote speaker: Dr. Theodore Roseman, former CRS President and VP at Baxter                                                  

Title: Heparin: Unraveling the Mystery

Chicago Rm A

9:30 9:35 Break Floor

9:35

10:20

Dr. Barrett Rabinow, Baxter Healthcare                                                              

Title: Nanoparticles-Impact on PK and Distribution

Chicago Rm A

10:20

11:05

Dr. Joseph Wong, Baxter Healthcare                                                                  

Title: Product Development Considerations with Injectable Nanosuspensions

Chicago Rm A

11:05

1:00

Poster presentation & Luncheon/Round Table Discussion

 

Chicago Rm B

1:15

2:00

Dr. William Mieler, University of Illinois at Chicago

Title: Thermo-responsive Hydrogels as a New Platform for Drug Delivery to the Posterior Segment of the Eye

Chicago Rm A

2:00

2:45

Dr. Michael Kaminski, Argonne National Laboratory

Title: Magnetic drug delivery technology

Chicago Rm A

2:45 2:50 Break Floor

2:50

3:35

Dr. Lonnie Shea, Northwestern University                                                                     

Title: Biomaterials for delivery of gene therapy vectors in regenerative medicine

Chicago Rm A

3:35 3:50 Presentation of Gift for Speakers, Poster Presentation Prize Awarded Chicago Rm A

3:50

3:55

Closing symposium remarks: Dr. Richard A. Gemeinhart, CRS -- Illinois Student Chapter Faculty Advisor

 

Chicago Rm A

3:55

3:57

Closing symposium remarks: Misuk Bae, Chair, CRS -- Illinois Student Chapter

 

Chicago Rm A